Partner with Daye to expand access to women's health diagnostics

Partner with Daye to expand access to women's health diagnostics

Clinical-grade, at-home testing for HPV, STIs, vaginal health, and hormones. Trusted by healthcare providers nationwide.

99.2% valid result rate

Comparable diagnostic accuracy to clinician-collected sampling, with significantly higher conclusive result rates in clinical trials.

Why providers choose Daye

Clinical-Grade Accuracy

FDA 510(k) cleared menstrual tampon and validated in peer-reviewed studies. Our at-home collection methods match or exceed traditional clinic-based testing performance.

Seamless Integration

Patients test at home, and results return to your dashboard in 3-5 days—with clinical recommendations included.

Improved Patient Access

Remove barriers to screening. Our at-home solutions increase testing uptake by 40-60%, particularly among underserved or underscreened populations.

“We’ve found that patients are far more comfortable using a tampon-based collection method compared to swabs. This has improved adherence and reduced the number of insufficient samples, which ultimately speeds up treatment timelines.”

How it works

How it works

1

Standardised self-collection using the medical-grade Diagnostic Tampon.

Standardised self-collection using the medical-grade Diagnostic Tampon.

2

Sample shipped with a stabilised transport medium suitable for PCR-based analysis.

Sample shipped with a stabilised transport medium suitable for PCR-based analysis.

3

Processing in accredited laboratories using validated qPCR assays.

Processing in accredited laboratories using validated qPCR assays.

4

Clinician-interpretable results with high conclusive rates and integration options for care pathways.

Clinician-interpretable results with high conclusive rates and integration options for care pathways.

Evidence highlights

Evidence highlights

HPV diagnostic accuracy

In a head-to-head comparison, the Diagnostic Tampon showed 82.9% sensitivity, 91.6% specificity, and a 99.2% conclusive result rate, performing comparably to clinician-collected samples and outperforming vaginal self-swabs.

STI detection

Across comparative studies, the tampon showed high concordance with clinician-collected samples for Chlamydia trachomatis, Neisseria gonorrhoeae, and Bacterial Vaginosis.

Microbiome Profiling

Tampon-based sampling generated more abundant microbial DNA—significantly increasing total bacterial mass and key taxa such as Lactobacillus and Ureaplasma.

Patient Acceptability

Across multiple cohorts, the majority of participants were willing to provide tampon samples, with a strong preference over both speculum exams and vaginal swabs, including among first-time screeners and those with GSM-related discomfort.

One tampon, multiple panels

The higher analyte yield from tampon sampling enables HPV, STI, and microbiome analysis from a single specimen, reducing patient burden and improving workflow efficiency.

99.2%

Conclusive HPV result rate in the STAMP accuracy study

100%

Willingness to provide a tampon sample across multiple cohorts

0%

Positive agreement for Gonorrhoea & BV in paired comparisons

Partner with us to transform women's healthcare

Partner with us to transform women's healthcare

© 2026 Daye Biotech Ltd, 4th Floor, 22 Southwark Bridge Road,

London SE1 9HF, UK

Operated by Anne's Day Ltd, a company registered in England and Wales (Co. No. 11044785) 4th Floor 22 Southwark Bridge Road, London, United Kingdom, SE1 9HF. Anne's Day Ltd is a wholly-owned subsidiary of Daye Biotech Ltd (Ireland, Co. No. 788588), Pavilion House, 31 Fitzwilliam Square, Dublin 2, D02 F403.
The Daye Diagnostic Tampon is a UKCA- and CE-marked medical device, manufactured under ISO 13485 and GMP, for self-collection of vaginal samples analysed by UKAS-accredited (ISO 15189) partner laboratories. Daye services are not intended to diagnose, treat, cure, or prevent disease in isolation; HPV, STI, and hormone results require interpretation by a qualified healthcare professional. Information on this site is educational and not a substitute for medical advice. This site is directed at users in the United Kingdom. Products, services, indications, regulatory status, and clinical claims described here apply to the UK only and may differ in other jurisdictions.

© 2026 Daye Limited, 4th Floor, 22 Southwark Bridge Road, London SE1 9HF, UK

Operated by Anne's Day Ltd, a company registered in England and Wales (Co. No. 11044785) 4th Floor 22 Southwark Bridge Road, London, United Kingdom, SE1 9HF. Anne's Day Ltd is a wholly-owned subsidiary of Daye Biotech Ltd (Ireland, Co. No. 788588), Pavilion House, 31 Fitzwilliam Square, Dublin 2, D02 F403.
The Daye Diagnostic Tampon is a UKCA- and CE-marked medical device, manufactured under ISO 13485 and GMP, for self-collection of vaginal samples analysed by UKAS-accredited (ISO 15189) partner laboratories. Daye services are not intended to diagnose, treat, cure, or prevent disease in isolation; HPV, STI, and hormone results require interpretation by a qualified healthcare professional. Information on this site is educational and not a substitute for medical advice. This site is directed at users in the United Kingdom. Products, services, indications, regulatory status, and clinical claims described here apply to the UK only and may differ in other jurisdictions.

© 2026 Daye Biotech Ltd, 4th Floor, 22 Southwark Bridge Road,

London SE1 9HF, UK

Operated by Anne's Day Ltd, a company registered in England and Wales (Co. No. 11044785) 4th Floor 22 Southwark Bridge Road, London, United Kingdom, SE1 9HF. Anne's Day Ltd is a wholly-owned subsidiary of Daye Biotech Ltd (Ireland, Co. No. 788588), Pavilion House, 31 Fitzwilliam Square, Dublin 2, D02 F403.
The Daye Diagnostic Tampon is a UKCA- and CE-marked medical device, manufactured under ISO 13485 and GMP, for self-collection of vaginal samples analysed by UKAS-accredited (ISO 15189) partner laboratories. Daye services are not intended to diagnose, treat, cure, or prevent disease in isolation; HPV, STI, and hormone results require interpretation by a qualified healthcare professional. Information on this site is educational and not a substitute for medical advice. This site is directed at users in the United Kingdom. Products, services, indications, regulatory status, and clinical claims described here apply to the UK only and may differ in other jurisdictions.